1. Academic Validation
  2. Development of 18F-labeled picolinamide probes for PET imaging of malignant melanoma

Development of 18F-labeled picolinamide probes for PET imaging of malignant melanoma

  • J Med Chem. 2013 Feb 14;56(3):895-901. doi: 10.1021/jm301740k.
Hongguang Liu 1 Shuanglong Liu Zheng Miao Zixin Deng Baozhong Shen Xuechuan Hong Zhen Cheng
Affiliations

Affiliation

  • 1 Molecular Imaging Program at Stanford (MIPS), Bio-X Program, Department of Radiology, Stanford University, California, 94305-5344, USA.
Abstract

Melanoma is an aggressive skin Cancer with worldwide increasing incidence. Development of positron emission tomography (PET) probes for early detection of melanoma is critical for improving the survival rate of melanoma patients. In this research, (18)F-picolinamide-based PET probes were prepared by direct radiofluorination of the bromopicolinamide precursors using no-carrier-added (18)F-fluoride. The resulting probes, (18)F-1, (18)F-2 and (18)F-3, were then evaluated in vivo by small animal PET imaging and biodistribution studies in C57BL/6 mice bearing B16F10 murine melanoma tumors. Noninvasive small animal PET studies demonstrated excellent tumor imaging contrasts for all probes, while (18)F-2 showed higher tumor to muscle ratios than (18)F-1 and (18)F-3. Furthermore, (18)F-2 demonstrated good in vivo stability as evidenced by the low bone uptake in biodistribution studies. Collectively, these findings suggest (18)F-2 as a highly promising PET probe for translation into clinical detection of melanoma.

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